首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Purification and restriction endonuclease mapping of soybean 18 S and 25 S ribosomal RNA genes
Authors:Harald Friedrich  Vera Hemleben  Richard B Meagher  Joe L Key
Institution:(1) Lehrstuhl für Genetik, Institut für Biologie II der Universität, Auf der Morgenstelle 28, D-7400 Tübingen, Federal Republic of Germany;(2) Department of Botany, University of Georgia, 30601 Athens, GA, USA
Abstract:The restriction endonuclease map of the 25 S and 18 S ribosomal RNA genes of a higher plant is presented. Soybean (Glycine max) rDNA was enriched by preparative buoyant density centrifugation in CsCl-actinomycin D gradients. The buoyant density of the rDNA was determined to be 1.6988 g cm–3 by analytical centrifugation in CsCl. Saturation hybridization showed that 0.1% of the total DNA contains 25 S and 18 S rRNA coding sequences. This is equivalent to 800 rRNA genes per haploid genome (DNA content: 1.29 pg) or 3200 for the tetraploid genome. Restriction endonuclease mapping was performed with Bam H I, Hind III, Eco R I, and BstI. The repeating unit of the soybean ribosomal DNA has a molecular weight of 5.9·106 or approximately 9,000 kb. The 25 S and 18 S rRNA coding sequences were localized within the restriction map of the repeating unit by specific hybridization with either 125I]25 S or 125I]18 S rRNA. It was demonstrated that there is no heterogeneity even in the spacer region of the soybean rDNA.
Keywords:Gene mapping  Glycine  Restriction enzymes  Ribosomal RNA genes
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号